Clinical Research Tech: Tobacco Dependence Trials

Indiana University; Indianapolis (IN); On-site; USD 42,000 - 56,000; Full time

Benefits offered by this job

Medical and dental insurance

Health savings account

Tuition subsidy for employees and/or a

Paid holidays

Paid time off

Employee assistance program

Job summary

Indiana University Indianapolis Campus is seeking an intermediate-level research support professional to assist in clinical studies. You will help coordinate screening, enrollment, data collection, and regulatory documentation, ensuring protocol adherence and quality.

This in-person role emphasizes communication with investigators and participants and may involve handling study materials and schedules. The position connects to tobacco-related research initiatives and offers benefits typical for

Qualifications

• High school diploma or GED plus 5 years patient-related or research experience including 2 years with clinical studies.
• Associate's degree in allied health with 1 year of patient-related or research experience.
• Bachelor's degree in any field or science/health-related field with related experience.

Responsibilities

• Assist in conducting clinical research studies following established protocols.
• Identify and recruit subjects; schedule per protocol; obtain consent and collect data.
• Coordinate study procedures; communicate with investigators and PI.
• Collect clinical samples and manage storage as needed.
• Assist with advertising and information for participant recruitment.
• Ensure documentation of Case Report Forms and regulatory documents; support audits.
• Maintain inventory and study supplies; assist with participant payments.

Skills

Written communication

Verbal communication

Professionalism

Time management

Quality focus

Flexibility

Dependable

Education

High school diploma or equivalent

Associate's degree in allied health

Bachelor's degree in any field

Bachelor's degree in science/health-related field

Job description

Indiana University Indianapolis Campus is seeking an intermediate-level research support professional to assist in clinical studies. You will help coordinate screening, enrollment, data collection, and regulatory documentation, ensuring protocol adherence and quality.

This in-person role emphasizes communication with investigators and participants and may involve handling study materials and schedules. The position connects to tobacco-related research initiatives and offers benefits typical for